Türk Kardiyoloji Derneği Arşivi (Dec 2019)

Treatment of Libman-Sacks endocarditis by combination of warfarin and immunosuppressive therapy

  • Mehmet Rasih Sonsöz,
  • Rukiye Dilara Tekin,
  • Ahmet Gül,
  • Zehra Buğra,
  • Dursun Atılgan

DOI
https://doi.org/10.5543/tkda.2019.29213
Journal volume & issue
Vol. 47, no. 8
pp. 687 – 690

Abstract

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Antiphospholipid syndrome (APS) is a clinical disorder that creates an increased risk of arterial or venous thrombotic events or pregnancy-associated complications and includes the presence of autoantibodies against negatively charged phospholipids. This syndrome is often associated with systemic autoimmune diseases, such as systemic lupus erythematosus (SLE). Libman-Sacks endocarditis is a form of non-bacterial thrombotic endocarditis and is infrequently seen in APS. There are few data documenting the echocardiographic response of APS valve disease to medical treatment. This is an unusual case of a young female patient with SLE and APS who had chorea and non-bacterial thrombotic aortic valve endocarditis. Echocardiography revealed that the vegetation had receded after a combination of warfarin and immunosuppressive therapy.

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